Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP492714.RA6__-yTxGsUd1h0O3au7M0_UoLMoz-RPM6L5Krlk1HF0130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP492714.RA6__-yTxGsUd1h0O3au7M0_UoLMoz-RPM6L5Krlk1HF0130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP492714.RA6__-yTxGsUd1h0O3au7M0_UoLMoz-RPM6L5Krlk1HF0130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP492714.RA6__-yTxGsUd1h0O3au7M0_UoLMoz-RPM6L5Krlk1HF0130_provenance.
- NP492714.RA6__-yTxGsUd1h0O3au7M0_UoLMoz-RPM6L5Krlk1HF0130_assertion description "[The association of mutations in RDS with retinitis pigmentosa indicates that ROM1 is a strong candidate gene for human retinopathies.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP492714.RA6__-yTxGsUd1h0O3au7M0_UoLMoz-RPM6L5Krlk1HF0130_provenance.
- NP492714.RA6__-yTxGsUd1h0O3au7M0_UoLMoz-RPM6L5Krlk1HF0130_assertion evidence source_evidence_literature NP492714.RA6__-yTxGsUd1h0O3au7M0_UoLMoz-RPM6L5Krlk1HF0130_provenance.
- NP492714.RA6__-yTxGsUd1h0O3au7M0_UoLMoz-RPM6L5Krlk1HF0130_assertion SIO_000772 1610568 NP492714.RA6__-yTxGsUd1h0O3au7M0_UoLMoz-RPM6L5Krlk1HF0130_provenance.
- NP492714.RA6__-yTxGsUd1h0O3au7M0_UoLMoz-RPM6L5Krlk1HF0130_assertion wasDerivedFrom befree-20140225 NP492714.RA6__-yTxGsUd1h0O3au7M0_UoLMoz-RPM6L5Krlk1HF0130_provenance.
- NP492714.RA6__-yTxGsUd1h0O3au7M0_UoLMoz-RPM6L5Krlk1HF0130_assertion wasGeneratedBy ECO_0000203 NP492714.RA6__-yTxGsUd1h0O3au7M0_UoLMoz-RPM6L5Krlk1HF0130_provenance.
- befree-20140225 importedOn "2014-02-25" NP492714.RA6__-yTxGsUd1h0O3au7M0_UoLMoz-RPM6L5Krlk1HF0130_provenance.